ExonSkipDB: functional annotation of exon skipping event in human

Gene summary for FOXP4

Gene summary

Gene information	Gene symbol	FOXP4
	Gene ID	116113
	Gene name	forkhead box P4
	Synonyms	hFKHLA
	Cytomap	6p21.1
	Type of gene	protein-coding
	Description	forkhead box protein P4fork head-related protein like Awinged-helix repressor FOXP4
	Modification date	20180522
	UniProtAcc	Q8IVH2
	Context	PubMed: FOXP4 [Title/Abstract] AND exon [Title/Abstract] AND skip [Title/Abstract] - Title (PMID)

Gene ontology of each this gene with evidence of Inferred from Direct Assay (IDA) from Entrez

Gene

GO ID

GO term

PubMed ID

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Exon skipping events across known transcript of Ensembl for FOXP4 from UCSC genome browser

Skipped exons in TCGA and GTEx based on Ensembl gene isoform structure.
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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Gene isoform structures and expression levels for FOXP4

Expression levels of gene isoforms across TCGA.

Expression levels of gene isoforms across GTEx.

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Exon skipping events with PSIs in TCGA for FOXP4

Information of exkip skipping event in TCGA.

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_451532	6	41533486:41533702:41545723:41545819:41552506:41552556	41545723:41545819	ENSG00000137166.10	ENST00000373060.1,ENST00000409208.1,ENST00000307972.4,ENST00000373063.3,ENST00000373057.3
exon_skip_451536	6	41545723:41545819:41552506:41552629:41553168:41553255	41552506:41552629	ENSG00000137166.10	ENST00000373060.1,ENST00000409208.1,ENST00000307972.4,ENST00000373063.3
exon_skip_451541	6	41553174:41553255:41554746:41554894:41555036:41555250	41554746:41554894	ENSG00000137166.10	ENST00000373060.1,ENST00000409208.1,ENST00000307972.4,ENST00000373057.3
exon_skip_451550	6	41557508:41557592:41557700:41557908:41558008:41558085	41557700:41557908	ENSG00000137166.10	ENST00000373060.1,ENST00000307972.4,ENST00000373057.3
exon_skip_451551	6	41557508:41557592:41557736:41557908:41558008:41558085	41557736:41557908	ENSG00000137166.10	ENST00000409208.1,ENST00000373063.3
exon_skip_451552	6	41558008:41558085:41558958:41559060:41562607:41562729	41558958:41559060	ENSG00000137166.10	ENST00000373060.1,ENST00000409208.1,ENST00000307972.4,ENST00000373063.3,ENST00000373057.3
exon_skip_451554	6	41562607:41562729:41564913:41564980:41565518:41565688	41564913:41564980	ENSG00000137166.10	ENST00000373060.1,ENST00000409208.1,ENST00000307972.4,ENST00000373063.3,ENST00000373057.3
exon_skip_451556	6	41564913:41564980:41565518:41565688:41566526:41567697	41565518:41565688	ENSG00000137166.10	ENST00000373060.1,ENST00000409208.1,ENST00000307972.4,ENST00000373063.3,ENST00000373057.3

PSI values of skipped exons in TCGA.

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Exon skipping events with PSIs in GTEx for FOXP4

Information of exkip skipping event in GTEx

Exon skip ID	chr	Exons involved in exon skipping	Skipped exon	ENSG	ENSTs
exon_skip_451532	6	41533486:41533702:41545723:41545819:41552506:41552556	41545723:41545819	ENSG00000137166.10	ENST00000373063.3,ENST00000373060.1,ENST00000409208.1,ENST00000373057.3,ENST00000307972.4
exon_skip_451536	6	41545723:41545819:41552506:41552629:41553168:41553255	41552506:41552629	ENSG00000137166.10	ENST00000373063.3,ENST00000373060.1,ENST00000409208.1,ENST00000307972.4
exon_skip_451541	6	41553174:41553255:41554746:41554894:41555036:41555250	41554746:41554894	ENSG00000137166.10	ENST00000373060.1,ENST00000409208.1,ENST00000373057.3,ENST00000307972.4
exon_skip_451550	6	41557508:41557592:41557700:41557908:41558008:41558085	41557700:41557908	ENSG00000137166.10	ENST00000373060.1,ENST00000373057.3,ENST00000307972.4
exon_skip_451551	6	41557508:41557592:41557736:41557908:41558008:41558085	41557736:41557908	ENSG00000137166.10	ENST00000373063.3,ENST00000409208.1
exon_skip_451552	6	41558008:41558085:41558958:41559060:41562607:41562729	41558958:41559060	ENSG00000137166.10	ENST00000373063.3,ENST00000373060.1,ENST00000409208.1,ENST00000373057.3,ENST00000307972.4
exon_skip_451554	6	41562607:41562729:41564913:41564980:41565518:41565688	41564913:41564980	ENSG00000137166.10	ENST00000373063.3,ENST00000373060.1,ENST00000409208.1,ENST00000373057.3,ENST00000307972.4

PSI values of skipped exons in GTEx.

* Skipped exon sequences.

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Open reading frame (ORF) annotation in the exon skipping event for FOXP4

Open reading frame (ORF) of individual exon skipping events in TCGA based on the Ensembl gene structure combined from isoforms.

ENST	Start of skipped exon	End of skipped exon	ORF
ENST00000307972	41554746	41554894	Frame-shift
ENST00000373060	41554746	41554894	Frame-shift
ENST00000307972	41557700	41557908	Frame-shift
ENST00000373060	41557700	41557908	Frame-shift
ENST00000307972	41564913	41564980	Frame-shift
ENST00000373060	41564913	41564980	Frame-shift
ENST00000307972	41565518	41565688	Frame-shift
ENST00000373060	41565518	41565688	Frame-shift
ENST00000307972	41545723	41545819	In-frame
ENST00000373060	41545723	41545819	In-frame
ENST00000307972	41552506	41552629	In-frame
ENST00000373060	41552506	41552629	In-frame
ENST00000307972	41558958	41559060	In-frame
ENST00000373060	41558958	41559060	In-frame

Open reading frame (ORF) of individual exon skipping events in GTEx based on the Ensembl gene structure combined from isoforms.

ENST	Start of skipped exon	End of skipped exon	ORF
ENST00000307972	41554746	41554894	Frame-shift
ENST00000373060	41554746	41554894	Frame-shift
ENST00000307972	41557700	41557908	Frame-shift
ENST00000373060	41557700	41557908	Frame-shift
ENST00000307972	41564913	41564980	Frame-shift
ENST00000373060	41564913	41564980	Frame-shift
ENST00000307972	41545723	41545819	In-frame
ENST00000373060	41545723	41545819	In-frame
ENST00000307972	41552506	41552629	In-frame
ENST00000373060	41552506	41552629	In-frame
ENST00000307972	41558958	41559060	In-frame
ENST00000373060	41558958	41559060	In-frame

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Infer the effects of exon skipping event on protein functional features for FOXP4

Exon skipping at the protein sequence level and followed lost functional features.
* Click on the image to enlarge it in a new window.

Loci of skipped exons in TCGA across genomic, transcript, and protein sequence levels of In-frame cases.

ENST	Length of mRNA	Length of AA seq.	Genomic start	Genomic end	mRNA start	mRNA end	AA start	AA end
ENST00000307972	3762	680	41545723	41545819	217	312	68	100
ENST00000373060	5965	680	41545723	41545819	663	758	68	100
ENST00000307972	3762	680	41552506	41552629	313	435	100	141
ENST00000373060	5965	680	41552506	41552629	759	881	100	141
ENST00000307972	3762	680	41558958	41559060	1447	1548	478	512
ENST00000373060	5965	680	41558958	41559060	1893	1994	478	512

Loci of skipped exons in GTEx across genomic, transcript, and protein sequence levels of In-frame cases.

ENST	Length of mRNA	Length of AA seq.	Genomic start	Genomic end	mRNA start	mRNA end	AA start	AA end
ENST00000307972	3762	680	41545723	41545819	217	312	68	100
ENST00000373060	5965	680	41545723	41545819	663	758	68	100
ENST00000307972	3762	680	41552506	41552629	313	435	100	141
ENST00000373060	5965	680	41552506	41552629	759	881	100	141
ENST00000307972	3762	680	41558958	41559060	1447	1548	478	512
ENST00000373060	5965	680	41558958	41559060	1893	1994	478	512

Lost protein functional features of individual exon skipping events in TCGA.

UniProt acc.	Start of exon skipping (AA)	End of exon skipping (AA)	Protein feature start (AA)	Protein feature end (AA)	Category of protein feature	Description of feature
Q8IVH2	68	100	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	68	100	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	68	100	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	68	100	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	68	100	86	86	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
Q8IVH2	68	100	86	86	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
Q8IVH2	100	141	141	142	Alternative sequence	ID=VSP_043034;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:15489334;Dbxref=PMID:15489334
Q8IVH2	100	141	141	142	Alternative sequence	ID=VSP_043034;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:15489334;Dbxref=PMID:15489334
Q8IVH2	100	141	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	100	141	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	100	141	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	100	141	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	478	512	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	478	512	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	478	512	467	559	DNA binding	Note=Fork-head;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU00089
Q8IVH2	478	512	467	559	DNA binding	Note=Fork-head;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU00089

Lost protein functional features of individual exon skipping events in GTEx.

UniProt acc.	Start of exon skipping (AA)	End of exon skipping (AA)	Protein feature start (AA)	Protein feature end (AA)	Category of protein feature	Description of feature
Q8IVH2	68	100	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	68	100	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	68	100	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	68	100	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	68	100	86	86	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
Q8IVH2	68	100	86	86	Modified residue	Note=Phosphoserine;Ontology_term=ECO:0000244;evidence=ECO:0000244\|PubMed:23186163;Dbxref=PMID:23186163
Q8IVH2	100	141	141	142	Alternative sequence	ID=VSP_043034;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:15489334;Dbxref=PMID:15489334
Q8IVH2	100	141	141	142	Alternative sequence	ID=VSP_043034;Note=In isoform 2. Missing;Ontology_term=ECO:0000303;evidence=ECO:0000303\|PubMed:15489334;Dbxref=PMID:15489334
Q8IVH2	100	141	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	100	141	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	100	141	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	100	141	65	219	Compositional bias	Note=Gln-rich
Q8IVH2	478	512	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	478	512	1	680	Chain	ID=PRO_0000091889;Note=Forkhead box protein P4
Q8IVH2	478	512	467	559	DNA binding	Note=Fork-head;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU00089
Q8IVH2	478	512	467	559	DNA binding	Note=Fork-head;Ontology_term=ECO:0000255;evidence=ECO:0000255\|PROSITE-ProRule:PRU00089

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SNVs in the skipped exons for FOXP4

- Lollipop plot for presenting exon skipping associated SNVs.
* Click on the image to enlarge it in a new window.

- Differential PSIs between mutated versus non-mutated samples.

FOXP4_BRCA_exon_skip_451550_psi_boxplot.png
boxplot

FOXP4_BRCA_exon_skip_451551_psi_boxplot.png
boxplot

FOXP4_COAD_exon_skip_451550_psi_boxplot.png
boxplot

FOXP4_COAD_exon_skip_451551_psi_boxplot.png
boxplot

FOXP4_STAD_exon_skip_451550_psi_boxplot.png
boxplot

FOXP4_STAD_exon_skip_451551_psi_boxplot.png
boxplot

- Non-synonymous mutations located in the skipped exons in TCGA.

Cancer type	Sample	ESID	Skipped exon start	Skipped exon end	Mutation start	Mutation end	Mutation type	Reference seq	Mutation seq	AAchange
UCEC	TCGA-BG-A0LX-01	exon_skip_451536	41552507	41552629	41552576	41552576	Frame_Shift_Del	C	-	p.P124fs
BRCA	TCGA-AQ-A04J-01	exon_skip_451550 exon_skip_451551	41557701	41557908	41557744	41557745	Frame_Shift_Del	TC	-	p.S399fs
BRCA	TCGA-AQ-A04J-01	exon_skip_451550 exon_skip_451551	41557737	41557908	41557744	41557745	Frame_Shift_Del	TC	-	p.S399fs
LIHC	TCGA-DD-A3A0-01	exon_skip_451550 exon_skip_451551	41557701	41557908	41557781	41557781	Frame_Shift_Del	C	-	p.H410fs
LIHC	TCGA-DD-A3A0-01	exon_skip_451550 exon_skip_451551	41557737	41557908	41557781	41557781	Frame_Shift_Del	C	-	p.H410fs
STAD	TCGA-HU-8602-01	exon_skip_451550 exon_skip_451551	41557701	41557908	41557781	41557781	Frame_Shift_Del	C	-	p.H410fs
STAD	TCGA-HU-8602-01	exon_skip_451550 exon_skip_451551	41557737	41557908	41557781	41557781	Frame_Shift_Del	C	-	p.H410fs
KIRC	TCGA-A3-3365-01	exon_skip_451554	41564914	41564980	41564917	41564921	Frame_Shift_Del	CCCCA	-	p.SPT554fs
LIHC	TCGA-DD-A1EG-01	exon_skip_451554	41564914	41564980	41564922	41564922	Frame_Shift_Del	C	-	p.T556fs
COAD	TCGA-AA-3663-01	exon_skip_451550 exon_skip_451551	41557701	41557908	41557780	41557781	Frame_Shift_Ins	-	C	p.H410fs
COAD	TCGA-AA-3663-01	exon_skip_451550 exon_skip_451551	41557737	41557908	41557780	41557781	Frame_Shift_Ins	-	C	p.H410fs
PRAD	TCGA-XK-AAIW-01	exon_skip_451532	41545724	41545819	41545742	41545742	Nonsense_Mutation	C	T	p.Q75*
UCEC	TCGA-B5-A11I-01	exon_skip_451550 exon_skip_451551	41557701	41557908	41557909	41557909	Splice_Site	G	A	e10+1
UCEC	TCGA-B5-A11I-01	exon_skip_451550 exon_skip_451551	41557701	41557908	41557909	41557909	Splice_Site	G	A	p.E453_splice
UCEC	TCGA-B5-A11I-01	exon_skip_451550 exon_skip_451551	41557737	41557908	41557909	41557909	Splice_Site	G	A	e10+1
UCEC	TCGA-B5-A11I-01	exon_skip_451550 exon_skip_451551	41557737	41557908	41557909	41557909	Splice_Site	G	A	p.E453_splice

- Depth of coverage in the three exons composing exon skipping event

Depth of coverage in three exons	Mutation description
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557701
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: p.E453_splice
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557737
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: p.E453_splice
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557701
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: e10+1
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557737
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: e10+1
exon_skip_451550_UCEC_TCGA-B5-A11I-01.png
exon_skip_451551_UCEC_TCGA-B5-A11I-01.png
	Sample: TCGA-AQ-A04J-01
	Cancer type: BRCA
	ESID: exon_skip_451551
	Skipped exon start: 41557701
	Skipped exon end: 41557908
	Mutation start: 41557744
	Mutation end: 41557745
	Mutation type: Frame_Shift_Del
	Reference seq: TC
	Mutation seq: -
	AAchange: p.S399fs
	Sample: TCGA-AQ-A04J-01
	Cancer type: BRCA
	ESID: exon_skip_451551
	Skipped exon start: 41557737
	Skipped exon end: 41557908
	Mutation start: 41557744
	Mutation end: 41557745
	Mutation type: Frame_Shift_Del
	Reference seq: TC
	Mutation seq: -
	AAchange: p.S399fs
exon_skip_451550_BRCA_TCGA-AQ-A04J-01.png
exon_skip_451551_BRCA_TCGA-AQ-A04J-01.png
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557701
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: p.E453_splice
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557737
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: p.E453_splice
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557701
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: e10+1
	Sample: TCGA-B5-A11I-01
	Cancer type: UCEC
	ESID: exon_skip_451551
	Skipped exon start: 41557737
	Skipped exon end: 41557908
	Mutation start: 41557909
	Mutation end: 41557909
	Mutation type: Splice_Site
	Reference seq: G
	Mutation seq: A
	AAchange: e10+1
exon_skip_451550_UCEC_TCGA-B5-A11I-01.png
exon_skip_451551_UCEC_TCGA-B5-A11I-01.png
	Sample: TCGA-AQ-A04J-01
	Cancer type: BRCA
	ESID: exon_skip_451551
	Skipped exon start: 41557701
	Skipped exon end: 41557908
	Mutation start: 41557744
	Mutation end: 41557745
	Mutation type: Frame_Shift_Del
	Reference seq: TC
	Mutation seq: -
	AAchange: p.S399fs
	Sample: TCGA-AQ-A04J-01
	Cancer type: BRCA
	ESID: exon_skip_451551
	Skipped exon start: 41557737
	Skipped exon end: 41557908
	Mutation start: 41557744
	Mutation end: 41557745
	Mutation type: Frame_Shift_Del
	Reference seq: TC
	Mutation seq: -
	AAchange: p.S399fs
exon_skip_451550_BRCA_TCGA-AQ-A04J-01.png
exon_skip_451551_BRCA_TCGA-AQ-A04J-01.png

- Non-synonymous mutations located in the skipped exons in CCLE.

Sample	Skipped exon start	Skipped exon end	Mutation start	Mutation end	Mutation type	Reference seq	Mutation seq	AAchange
TGBC11TKB_STOMACH	41545724	41545819	41545796	41545796	Frame_Shift_Del	A	-	p.K93fs
PCI4B_UPPER_AERODIGESTIVE_TRACT	41554747	41554894	41554856	41554859	Frame_Shift_Del	CCAA	-	p.PN207fs
HCC2218_MATCHED_NORMAL_TISSUE	41545724	41545819	41545727	41545727	Missense_Mutation	C	T	p.L70F
NCIBL209_MATCHED_NORMAL_TISSUE	41545724	41545819	41545727	41545727	Missense_Mutation	C	T	p.L70F
TE441T_SOFT_TISSUE	41545724	41545819	41545739	41545739	Missense_Mutation	C	T	p.R74W
TMK1_STOMACH	41545724	41545819	41545739	41545739	Missense_Mutation	C	G	p.R74G
SNU398_LIVER	41545724	41545819	41545740	41545740	Missense_Mutation	G	T	p.R74L
DU145_PROSTATE	41557701	41557908	41557786	41557786	Missense_Mutation	C	T	p.P412L
DU145_PROSTATE	41557737	41557908	41557786	41557786	Missense_Mutation	C	T	p.P412L
MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	41557701	41557908	41557804	41557804	Missense_Mutation	C	T	p.P418L
MOLT4_HAEMATOPOIETIC_AND_LYMPHOID_TISSUE	41557737	41557908	41557804	41557804	Missense_Mutation	C	T	p.P418L
NCIH2126_LUNG	41565519	41565688	41565675	41565675	Missense_Mutation	C	T	p.P628S
MFE296_ENDOMETRIUM	41557701	41557908	41557907	41557907	Splice_Site	A	G	p.S452S
MFE296_ENDOMETRIUM	41557737	41557908	41557907	41557907	Splice_Site	A	G	p.S452S

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Splicing Quantitative Trait Loci (sQTL) in the exon skipping event for FOXP4

sQTL information located at the skipped exons.

Exon skip ID

Chromosome

Three exons

Skippped exon

ENST

Cancer type

SNP id

Location

DNA change (ref/var)

P-value

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Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for FOXP4

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Survival analysis of Splicing Quantitative Trait Methylation (sQTM) in the skipped exon for FOXP4

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RelatedDrugs for FOXP4

Approved drugs targeting this gene.
(DrugBank Version 5.1.0 2018-04-02)

Gene

UniProtAcc

DrugBank ID

Drug name

Drug activity

Drug type

Drug status

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RelatedDiseases for FOXP4

Diseases associated with this gene.
(DisGeNet 4.0)

Gene	Disease ID	Disease name	# pubmeds	Source
FOXP4	C0033578	Prostatic Neoplasms	1	CTD_human

	Gene summary
	Gene structures and expression levels
	Exon skipping events with PSIs in TCGA
	Exon skipping events with PSIs in GTEx
	Open reading frame (ORF) annotation in the exon skipping event
	Exon skipping events in the canonical protein sequence
	SNVs in the skipped exons with depth of coverage
	Splicing Quantitative Trait Loci (sQTLs) in the skipped exons
	Splicing Quantitative Trait Methylation (sQTM) in the skipped exon
	Related drugs with this gene
	Related diseases with this gene

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